Rodríguez-Iturbe Bernardo, Vaziri Nosratola D, Herrera-Acosta Jaime, Johnson Richard J
Servicio de Nefrología, Hospital Universitario, Universidad del Zulia, Instituto de Inmunobiología (Fundacite-Zulia Maracaibo 400-A, Venezuela.
Am J Physiol Renal Physiol. 2004 Apr;286(4):F606-16. doi: 10.1152/ajprenal.00269.2003.
Recent evidence indicates that interstitial infiltration of T cells and macrophages plays a role in the pathogenesis of salt-sensitive hypertension. The present review examines this evidence and summarizes the investigations linking the renal accumulation of immune cells and oxidative stress in the development of hypertension. The mechanisms involved in the hypertensive effects of oxidant stress and tubulointerstitial inflammation, in particular intrarenal ANG II activity, are discussed, focusing on their potential for sodium retention. The possibility of autoimmune reactivity in hypertension is raised in the light of the proinflammatory and immunogenic pathways stimulated by the interrelationship between oxidant stress and inflammatory response. Finally, we present some clinical considerations derived from the recognition of this interrelationship.
最近的证据表明,T细胞和巨噬细胞的间质浸润在盐敏感性高血压的发病机制中起作用。本综述审视了这一证据,并总结了在高血压发展过程中,将免疫细胞在肾脏的积聚与氧化应激联系起来的研究。讨论了氧化应激和肾小管间质炎症(特别是肾内血管紧张素II活性)的高血压效应所涉及的机制,重点关注它们导致钠潴留的可能性。鉴于氧化应激与炎症反应之间的相互关系所刺激的促炎和免疫原性途径,提出了高血压中自身免疫反应性的可能性。最后,我们提出了一些基于对这种相互关系的认识而产生的临床思考。